We bought the Ampure DNA purification system. Would you be able to put it together, explore how it works, and give us training?
It might be worth taking a PCR product that is no longer needed but had a strong band (something that we already sequenced) and runningon a gel 10 5ul of the original, 2) 5ul Ampure cleaned-up version, and 3) 5ul MoBio cleaned version.
The sooner the better (within two or three weeks?), because I am imagining that Craig and possibly Tyler Dreaden might want to use it for the next MiSeq library.
For individual Sanger sequencing submission, we will still be using ExoSap. This is only for large volumes that have to be really clean, like whole library submissions.